User:Ahmed osama 2

ahmed osama abdo metwaly : now in 7/2009 work: chemistry section head in MEPACO in Egypt Ahmed Osama Abdo

28th Radi st. El-Zewiton- Cairo, Egypt. Tel      : 02-22599794 Mobil  : 0121875262 	Education : Certificate         : B.Sc. in Science, 1999, Ain Shames Univ. (Very Good ) □PERSONAL INFORMATIONS: 	Date of birth 	: 30/10/1978 	Age		: 29 Years 	Nationality    	: Egyptian 	Marital Status      : Married 	Language      	: Arabic (Native ) English (Fluent) German ( Fair ) 	 Religion    	: Muslim 	Military Service 	: Postponed 	Driving License   : Valid 	Computer Skills 	: Excellent Microsoft office (Word, Excel & Power point) Windows (98, 2000, Me & XP) Internet □Professional Experience : 	 Current job : - RM Unit Head in QC Department in MEPACO Pharmaceuticals. ( Arab Company For Pharmaceutical And Medicinal Plants; Egypt) From 1/2/2004 till now. - Consultant in MediFood Company in Chemistry Lab under license of MEPACO. - We are going now to have ISO17025, and I described as( Chemistry Quality Manger) for this project.

□Previous Jobs : 	Working in Cairo Lab in medical analysis from May 2000 till February 20001. 	Working in El-Nile Company for medicine & Chemical Industries as RM analyst from March 2001 till 5/2002. 	Working in ALKAN Pharma Company as RM analyst in QC Dept. & as purchasing specialist from 5/2002 till 2/2004.

Additional Jobs: -	Consultant in Western Pharma (in Obour City)from 2/2006 till 8/2006 in starting up the QC Dept. (Chemistry Lab.) for have the Ministry of Health license. -	Consultant in Mash Pharma (in Badr City) from 3/2007 till 7/2007 in starting up the QC Dept. (Chemistry Lab.) for have the Ministry of Health license in the pharmaceutical industry. -	From 3/2008 till now Consultant in MediFood Company in Chemistry Lab under license of MEPACO.

□Personal skills -	Self motivated, creative, hard worker with leading character and very     good communication Skills. -	Leadership.

□Professional skills □ Quality Control Department : -	Responsible for analysis of bulk, S.F. & F.P. -	Developing new methods of analysis of new products. -	Responsible for analysis in process control & product follow up. -	Responsible for documentation.. -	Registration: Producing & writing a complete file for new products including: Specifications of (R.M., F.P., M.O.A & C.O.A.). -	Very Good knowledge of GMP and GLP. -	Responsible for all RM files (including MOA & COA) handling and producing.

-	Can handle and work on :- 1-	H.P.T.L.C. "CAMAG" 2-	H.P.L.C. "SHIMADZU" 3-	H.P.L.C. "WATERS" 4-	I.R. "SHIMADZU" 5-	ATOMIC ABSORPTION "SHIMADZU" 6-	U.V. "SHIMADZU" 7-	G.C. "HP4890D" 8-	PHYSICAL INSRUMENTS: -	Moisture analyzer "sartorius" -	Conductivity meter "schott" -	Melting point "sanyo" -	Disintegrator "erweka" -	Friability tester "erwka" -	Refractometer "B&S" -	Polarimeter "B&S" -	Metrohm karlfisher titrator -	Metrohm potentiometric titrator -	Tablet tester "pharmtron"

□Training Courses :

1- Internal Course of "GMP". 2- Internal Course of GLP by consult of MEPACO PHARMA. 3- External Course of Course of "ANALYTICAL VALIDATION ". 4- External Course of Courses on:	- ISO 9001: 2000 - ISO 14001 - OHSAS 18001: 99 - Internal audit. 5- Training on H.P.L.C. ,I.R., U.V. and Atomic Absorbtion "SHIMADZU" by Henerich Company      by MR / HANY GAMEL. 6- External courses in ISO 17025 including all its skills(covering all its accreditation requirements), sharing all work schedule to have ISO 17025 Accreditation science 2/2008 till now. 7- Internal Course of microbiological analysis by consult of MEPACO PHARMA 8- Internal Course of calibration of instrumental by supplier of instrumental. 9- External Course in NearIR.

□Job performed in Q.C department In MEPACO PHARMA :

My Job description as R.M. Unit head: 1.	Checking on supervisor, senior analyst and sampler for (RM, intermediate, bulk, SF) units. 2.	Determination the schedule of work inside the unit and distribution of samples on the supervisor, senior analyst and analyst. 3.	Organization the daily working plan which receives from Q.C. manager, planning Dept. & QA. 4.	Review all analysts log books for recording and calculations for all samples (RM or Product). 5.	Responsible for reviewing R.M. retained samples to ensure the traceability application. 6.	Sharing with Q.C. manager and Head of section to originate the main plan for working inside the department.

Other tasks: 7.	Review all analysts in all tests technically. 8.	Approve or reject raw materials semi-finished and finished products after their analysis according to the approved specification. 9.	Control and follow the work of the chemical analysis and testing of R.M, bulk, S.F. and F.P. to insure the verification of the approved specification. 10.	Prepare the specification of the test methods and quality control procedures delivered from the Q.A. department. 11.	Perform the standard operating procedures concerning the lab. work.. 12.	Ensure that the appropriate calibrations and validations of the equipments and processes are done according to the calibration schedule. 13.	Check that all instruments and lab. services are well maintained. 14.	Prepare the annual forecasts of the lab. Supplies, chemical, equipments and other requirements. 15.	Review of: -Process batch records. -Master formula of the products Which are approved by Q.A.    16-Co-ordination with other departments: 1.	Production department. 2.	Quality assurance. 3.	Planning department. 4.	Purchasing department. 5.	Maintenance. 6.	Personnel department.